US4094640A - Method for processing biomaterials - Google Patents

Method for processing biomaterials Download PDF

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Publication number
US4094640A
US4094640A US05/764,541 US76454177A US4094640A US 4094640 A US4094640 A US 4094640A US 76454177 A US76454177 A US 76454177A US 4094640 A US4094640 A US 4094640A
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US
United States
Prior art keywords
sample
biomaterial
pressure vessel
water
pressure
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US05/764,541
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English (en)
Inventor
Georg Iwantscheff
Egmont Scheubeck
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Siemens AG
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Siemens AG
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Filing date
Publication date
Application filed by Siemens AG filed Critical Siemens AG
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/40—Concentrating samples
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/12—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using combustion
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/02—Food
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/40—Concentrating samples
    • G01N1/4044—Concentrating samples by chemical techniques; Digestion; Chemical decomposition
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/02—Food
    • G01N33/12—Meat; Fish

Definitions

  • This invention relates to the processing of biomaterials in general and more particularly to an improved method for finding metal traces in a biomaterial.
  • a moist sample of the biomaterial, particularly meat is pre-dried in a closed pressure vessel and subsequently burned in oxygen.
  • no ash is produced which needs to be digested, but only gaseous and liquid products, the latter consisting of the condensate of the drying and combustion processes.
  • this condensate all the traces to be determined are quantitatively present, quasi-dissolved in its own juice.
  • the drying is continued to a residual moisture of 5 to 10%.
  • Particularly good data could be obtained if 20 to 30 g of the biomaterial with a water content of 70 to 90% were used.
  • the pre-drying usually takes place at 20 mbar and 110° C.
  • the combustion is particularly favorable at an oxygen pressure of 30 to 40 bar.
  • a 20 g sample of the biomaterial with a water content of 80% can be pre-dried in a closed pressure vessel at a pressure of about 20 mbar to a residual moisture of 5 to 10% in less than 30 minutes and subsequently be burned in oxygen at 30 to 40 bar.
  • a spherical processing vessel such as a Berthelot calorimetric bomb with external cooling has been found particulary well suited.
  • the water vapor produced in the drying of the biomaterial is preferably condensed to a large extent at the wall of the closed pressure vessel, which is cooled to about 10° C.
  • the combustion is preferably accomplished by an ignition device.
  • the metal traces can be determined from the process solution without the addition of chemicals. They can also be precipitated out by a complex former in a special precipitation and filtering apparatus. The precipitate can be presented by filtration on a diaphragm filter in a form suitable for the analysis.
  • biomaterials in particular meat
  • biomaterials in particular meat
  • trace metals can be determined from the solution obtained, in which the unknown metals are present, by means of X-ray fluorescence analysis.
  • the numerical results of blank tests obtained here are understandably very low.
  • a closed vessel suitable for implementing the method according to the present invention is preferably vertically disposed.
  • the processing vessel may consist of chromium-nickel-molybdenum steel and has a cooling device for its outer surface.
  • the sample is dried in the processing vessel, for instance, by high frequency induction heating, but mainly by resistance heating.
  • the shape of the heater is matched to the shape of the base area of the sample container.
  • the ignition for burning the sample material is provided either by an incandescent wire of platinum or by means of a high voltage spark.
  • a sample of 20 to 30 g of the biomaterial to be examined, with about 80% moisture can be comminuted, if desired, for homogenizing.
  • the comminuted sample is placed into a processing vessel equipped with a removable lid and external cooling in a sample container of quartz and, while being heated, is dried in the closed vessel.
  • the wall can be cooled during the drying.
  • pure oxygen is admitted and caused to fill the vessel up to 40 bar pressure and subsequently, the combusion takes place.
  • the trace elements, poisons and the like can be determined analytically from the removed process solution.
  • traces of metallic poisons such as, in particular, mercury, cadmium, lead and arsenic, in biomaterials can be determined if they are present in the order of magnitude from 10 -4 to 10 -6 %. It is also suited for determining other elements by known analytical methods such as atomic absorption spectrophotometry, colorimetry or polarography.
  • the drawing is a schematic longitudinal cross section of a processing vessel according to the present invention for biomaterial, particularly meat.
  • the processing vessel 20 is equipped with a fast closing lid 1.
  • the processing vessel is cooled by means of a cooling coil or a cooling jacket 10.
  • An ignition wire 11 is also disposed in the vessel.
  • a sample container 14 of quartz rests on a heater 13 by means of a mounting 12.
  • the biomaterial 15 is covered with a filter paper 16.
  • the solution, which collects at the bottom of the processing vessel after the method according to the present invention is carried out, is designated 17.
  • Two electrical grounding points 18 and 19 for the heater and the incandescent wire are also shown.
  • the collected process solution is placed together with the rinsing liquid in a 50 ml measuring flask and the latter is filled up with water to the 50 ml.
  • the time required for the processing of a sample is about 10 to 15 minutes if two processing equipments are used alternatingly.
  • the trace elements cadmium, mercury, arsenic and lead can easily be detected from the process solution.
  • the sample container 14 To 5 g of animal or vegetable fat i.e. a biomaterial which is essentially water-free (containing no more than 1-2% water), in the sample container 14 about 1 ml of distilled water is added and the sample is covered with filter paper 16. 9 ml of distilled water are placed in the bottom part of the processing apparatus and the latter is closed. After the external cooling is started, the apparatus is evacuated to about 20 mbar and pre-drying is effected for a few minutes with the resistance heater 13 by evaporating the water in the sample container. The heater is then switched off and the biomaterial is burned in oxygen at about 40 bar. After the processing, the metal traces can be determined analytically in the solution in the bottom part of the processing equipment as in Examples 1 and 2.

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • Molecular Biology (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
  • Investigating Or Analyzing Materials Using Thermal Means (AREA)
US05/764,541 1976-02-12 1977-01-31 Method for processing biomaterials Expired - Lifetime US4094640A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2605560A DE2605560C3 (de) 1976-02-12 1976-02-12 Aufschlußverfahren für Biomaterialien
DT2605560 1976-02-12

Publications (1)

Publication Number Publication Date
US4094640A true US4094640A (en) 1978-06-13

Family

ID=5969707

Family Applications (1)

Application Number Title Priority Date Filing Date
US05/764,541 Expired - Lifetime US4094640A (en) 1976-02-12 1977-01-31 Method for processing biomaterials

Country Status (10)

Country Link
US (1) US4094640A (de)
JP (1) JPS5299881A (de)
AT (1) AT352084B (de)
BE (1) BE851348A (de)
CH (1) CH600323A5 (de)
DE (1) DE2605560C3 (de)
FR (1) FR2341140A1 (de)
GB (1) GB1533691A (de)
IT (1) IT1085206B (de)
NL (1) NL7613327A (de)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4192849A (en) * 1977-11-28 1980-03-11 Siemens Aktiengesellschaft Pressure digester
US4879246A (en) * 1986-11-03 1989-11-07 Tessek Sdruzeni Praha Method and device for mineralization of carbonaceous material
EP1840561A3 (de) * 2006-03-30 2008-12-03 SII Nano Technology Inc. Vorrichtung zur Analyse fluoreszenter Röntgenstrahlen
US8252917B2 (en) 2003-10-24 2012-08-28 Selexis S.A. High efficiency gene transfer and expression in mammalian cells by a multiple transfection procedure of MAR sequences
US20130134157A1 (en) * 2011-11-30 2013-05-30 Michael R. Knox Single mode microwave device for producing exfoliated graphite
CN105136790A (zh) * 2015-09-03 2015-12-09 黑龙江大庄园肉业有限公司 一种牛肉汞含量的检测方法
RU2738166C1 (ru) * 2020-05-26 2020-12-09 Федеральное бюджетное учреждение науки "Федеральный научный центр медико-профилактических технологий управления рисками здоровью населения" Федеральной службы по надзору в сфере защиты прав потребителей и благополучия человека (ФБУН "ФНЦ медико-профилактических технологий управления рисками здоровью Способ измерений массовых концентраций мышьяка, кадмия, свинца, ртути в мясных и мясосодержащих продуктах методом масс-спектрометрии с индуктивно связанной плазмой

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3818697A1 (de) * 1988-06-01 1989-12-07 Jasper B V Heizgeraet zum erhitzen von probenmaterial in probenbehaeltern

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1247998A (en) * 1916-08-04 1917-11-27 Samuel W Parr Adiabatic calorimeter.
US3485565A (en) * 1967-05-16 1969-12-23 Packard Instrument Co Inc Combustion apparatus,particularly for preparation of samples for radioactive isotope tracer studies
US3542121A (en) * 1967-05-16 1970-11-24 Packard Instrument Co Inc Heat exchanging method for fluid material containing condensible vapor
US3665761A (en) * 1967-06-08 1972-05-30 Univ Georgetown Liquid vaporization calorimeter
US3844716A (en) * 1971-12-01 1974-10-29 Nuclear Chicago Corp Combustion method apparatus for preparing samples for liquid scintillation counting

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1247998A (en) * 1916-08-04 1917-11-27 Samuel W Parr Adiabatic calorimeter.
US3485565A (en) * 1967-05-16 1969-12-23 Packard Instrument Co Inc Combustion apparatus,particularly for preparation of samples for radioactive isotope tracer studies
US3542121A (en) * 1967-05-16 1970-11-24 Packard Instrument Co Inc Heat exchanging method for fluid material containing condensible vapor
US3665761A (en) * 1967-06-08 1972-05-30 Univ Georgetown Liquid vaporization calorimeter
US3844716A (en) * 1971-12-01 1974-10-29 Nuclear Chicago Corp Combustion method apparatus for preparing samples for liquid scintillation counting

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
B. Morsches et al, J. Anal. Chem., vol. 219, pp. 61-68, 1966. *
C.E. Gleit et al, Anal. Chem., vol. 34, No. 11, pp. 1454-1457, Oct. 1962. *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4192849A (en) * 1977-11-28 1980-03-11 Siemens Aktiengesellschaft Pressure digester
US4879246A (en) * 1986-11-03 1989-11-07 Tessek Sdruzeni Praha Method and device for mineralization of carbonaceous material
US8252917B2 (en) 2003-10-24 2012-08-28 Selexis S.A. High efficiency gene transfer and expression in mammalian cells by a multiple transfection procedure of MAR sequences
US9879297B2 (en) 2003-10-24 2018-01-30 Selexis Sa High efficiency gene transfer and expression in mammalian cells by amultiple transfection procedure of MAR sequences
US10669562B2 (en) 2003-10-24 2020-06-02 Selexis S.A. High efficiency gene transfer and expression in mammalian cells by a multiple transfection procedure of MAR sequences
EP1840561A3 (de) * 2006-03-30 2008-12-03 SII Nano Technology Inc. Vorrichtung zur Analyse fluoreszenter Röntgenstrahlen
US20130134157A1 (en) * 2011-11-30 2013-05-30 Michael R. Knox Single mode microwave device for producing exfoliated graphite
US20170240427A1 (en) * 2011-11-30 2017-08-24 Michael R. Knox Single mode microwave device for producing exfoliated graphite
US9763287B2 (en) * 2011-11-30 2017-09-12 Michael R. Knox Single mode microwave device for producing exfoliated graphite
CN105136790A (zh) * 2015-09-03 2015-12-09 黑龙江大庄园肉业有限公司 一种牛肉汞含量的检测方法
CN105136790B (zh) * 2015-09-03 2018-02-09 黑龙江大庄园肉业有限公司 一种牛肉汞含量的检测方法
RU2738166C1 (ru) * 2020-05-26 2020-12-09 Федеральное бюджетное учреждение науки "Федеральный научный центр медико-профилактических технологий управления рисками здоровью населения" Федеральной службы по надзору в сфере защиты прав потребителей и благополучия человека (ФБУН "ФНЦ медико-профилактических технологий управления рисками здоровью Способ измерений массовых концентраций мышьяка, кадмия, свинца, ртути в мясных и мясосодержащих продуктах методом масс-спектрометрии с индуктивно связанной плазмой

Also Published As

Publication number Publication date
DE2605560B2 (de) 1979-01-04
FR2341140A1 (fr) 1977-09-09
DE2605560C3 (de) 1979-08-30
IT1085206B (it) 1985-05-28
GB1533691A (en) 1978-11-29
AT352084B (de) 1979-08-27
JPS5299881A (en) 1977-08-22
DE2605560A1 (de) 1977-08-18
ATA930876A (de) 1979-02-15
CH600323A5 (de) 1978-06-15
BE851348A (fr) 1977-05-31
FR2341140B1 (de) 1981-07-10
NL7613327A (nl) 1977-08-16

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